Nonaqueous electrolyte secondary battery

ABSTRACT

A nonaqueous electrolyte secondary battery according to an embodiment includes a spirally wound electrode body in which a positive electrode and a negative electrode are spirally wound with a separator interposed therebetween. The negative electrode includes a negative electrode current collector, a first negative electrode mixture layer disposed on a first surface of the negative electrode current collector, and a second negative electrode mixture layer disposed on a second surface of the negative electrode current collector. The first surface and the second surface face outward and inward of the electrode body, respectively. At least the first negative electrode mixture layer includes a Si active material. The content of the Si active material in terms of Si in the second negative electrode mixture layer is lower than the content of the Si active material in terms of Si in the first negative electrode mixture layer.

TECHNICAL FIELD

The present disclosure relates to a nonaqueous electrolyte secondarybattery and specifically to a nonaqueous electrolyte secondary batterythat includes a spirally wound electrode body.

BACKGROUND ART

It is known that Si and Si-containing materials are capable of occludinga larger amount of lithium ions per unit volume than carbon materials,such as graphite. Therefore, using a Si-containing material or the likeas a negative electrode active material increases the battery capacity.For example, PTL 1 discloses a nonaqueous electrolyte secondary batteryproduced using graphite and a Si-containing material as negativeelectrode active materials. PTL 1 also discloses a structure in whichthe mass ratio of the graphite to the Si-containing material in anegative electrode mixture layer (Mass of graphite/Mass of Si-containingmaterial) increases continuously or discontinuously with the distancefrom the surface of the negative electrode current collector.

CITATION LIST Patent Literature

PTL 1: Japanese Published Unexamined Patent Application No. 2013-178913

SUMMARY OF INVENTION Technical Problem

Since the volumes of Si and Si-containing materials change significantlyduring charging and discharging, the cycle characteristics of anonaqueous electrolyte secondary battery produced using a Si activematerial composed of at least one of Si and a Si-containing material asa negative electrode active material is likely to become degraded. Inparticular, in the case where the nonaqueous electrolyte secondarybattery includes a spirally wound electrode body, the change in thevolume of the Si active material greatly affects a portion of thenegative electrode which has a small radius of curvature, such as awinding start-side edge of the negative electrode from which theelectrode body is wound. An object of the present disclosure is toenhance the cycle characteristics of a nonaqueous electrolyte secondarybattery including a spirally wound electrode body produced using a Siactive material as a negative electrode active material.

Solution to Problem

A nonaqueous electrolyte secondary battery according to an embodiment ofthe present disclosure is a nonaqueous electrolyte secondary batteryincluding a spirally wound electrode body including in which a positiveelectrode and a negative electrode are spirally wound with a separatorinterposed therebetween. The negative electrode includes a negativeelectrode current collector, a first negative electrode mixture layerdisposed on a first surface of the negative electrode current collector,and a second negative electrode mixture layer disposed on a secondsurface of the negative electrode current collector, the first surfaceand the second surface facing outward and inward of the electrode body,respectively. The first negative electrode mixture layer includes a Siactive material composed of at least one of Si and a Si-containingmaterial. The content of the Si active material in terms of Si in thesecond negative electrode mixture layer is lower than the content of theSi active material in terms of Si in the first negative electrodemixture layer.

Advantageous Effects of Invention

According to an aspect of the present disclosure, the cyclecharacteristics of a nonaqueous electrolyte secondary battery includinga spirally wound electrode body produced using a Si active material as anegative electrode active material may be enhanced.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a cross-sectional view of a nonaqueous electrolyte secondarybattery according to an embodiment.

FIG. 2 is a cross-sectional view of a negative electrode according to anembodiment.

DESCRIPTION OF EMBODIMENTS

As described above, the cycle characteristics of a nonaqueouselectrolyte secondary battery including a spirally wound electrode bodyproduced using a Si active material as a negative electrode activematerial is likely to become degraded. The degradation of cyclecharacteristics is caused due to a significant change in the volume ofthe Si active material which occurs during charging and discharging.Specifically, it is considered that the degradation of cyclecharacteristics be caused primarily because the significant change inthe volume of the Si active material results in the degradation or lossof the contact between active material particles and consequentlyincreases the amount of active material particles isolated from theelectrical conduction paths present in the negative electrode mixturelayer. In the case where a spirally wound electrode body is used, thechange in the volume of the Si active material greatly affects a portionof the negative electrode which has a small radius of curvature, such asa winding start-side edge of the negative electrode from which theelectrode body is wound.

The inventors of the present invention conducted extensive studies inorder to achieve the above object and consequently found that adjustingthe content of the Si active material in terms of Si in the secondnegative electrode mixture layer to be lower than the content of the Siactive material in terms of Si in the first negative electrode mixturelayer may markedly enhance the cycle characteristics of the battery. Inthe nonaqueous electrolyte secondary battery according to the presentdisclosure, the degradation of cycle characteristics may be limitedwhile a Si active material is added to a negative electrode mixturelayer with efficiency in order to increase battery capacity.

An embodiment of the present disclosure is described in detail below.Although the battery described below as an example is a cylindricalbattery that includes a spirally wound electrode body 14 and acylindrical battery casing 15 housing the spirally wound electrode body14, the shape of the battery casing is not limited to cylindrical andmay be, for example, rectangular. A battery casing composed of alaminated sheet including a metal layer and a resin layer may also beused. The electrode body may be any electrode body having a spirallywound structure. Although the electrode body may be formed in a flatshape, the structure of the negative electrode according to the presentdisclosure may be particularly effective when the electrode body has acylindrical, spirally wound structure.

FIG. 1 is a cross-sectional view of a nonaqueous electrolyte secondarybattery 10 according to an embodiment. As illustrated in FIG. 1 as anexample, the nonaqueous electrolyte secondary battery 10 includes aspirally wound electrode body 14, a nonaqueous electrolyte (notillustrated in the drawing), and a battery casing 15 that houses theelectrode body 14 and the nonaqueous electrolyte. The electrode body 14has a spirally wound structure in which a positive electrode 11 and anegative electrode 12 are spirally wound with a separator 13 interposedtherebetween. The battery casing 15 includes a closed-end, tubularpackaging can 16 and a sealing material 17 with which the opening of thepackaging can 16 is sealed. The nonaqueous electrolyte secondary battery10 further includes a resin gasket 28 interposed between the packagingcan 16 and the sealing material 17.

The nonaqueous electrolyte includes a nonaqueous solvent and anelectrolyte salt dissolved in the nonaqueous solvent. Examples of thenonaqueous solvent include an ester, an ether, a nitrile, an amide, andmixed solvents of two or more of the above solvents. The nonaqueoussolvent may include a halogen-substituted compound produced by replacingat least a part of the hydrogen atoms included in any of the abovesolvents with halogen atoms, such as fluorine atoms. The nonaqueouselectrolyte is not limited to a liquid electrolyte and may be a solidelectrolyte including a gelatinous polymer or the like. Examples of theelectrolyte salt include lithium salts, such as LiPF₆.

The electrode body 14 is constituted by a long-length positive electrode11, a long-length negative electrode 12, two long-length separators 13,a positive electrode tab 20 joined to the positive electrode 11, and anegative electrode tab 21 joined to the negative electrode 12. Thenegative electrode 12 is formed to be a size larger than the positiveelectrode 11 in order to prevent the precipitation of lithium.Specifically, the negative electrode 12 is formed so as to be longerthan the positive electrode 11 in the longitudinal direction and thewidth direction (transverse direction). The two separators 13 are formedto be a size larger than at least the positive electrode 11 and arrangedsuch that, for example, the positive electrode 11 is interposedtherebetween.

Insulating plates 18 and 19 are disposed above and below the electrodebody 14, respectively. In the example illustrated in FIG. 1, thepositive electrode tab 20 attached to the positive electrode 11 extendstoward the sealing material 17 through a through-hole formed in theinsulating plate 18, and the negative electrode tab 21 attached to thenegative electrode 12 extends toward the bottom of the packaging can 16through the outside of the insulating plate 19. The positive electrodetab 20 is connected to the lower surface of a bottom plate 23 of thesealing material 17 by welding or the like. A cap 27, which is the topplate of the sealing material 17 electrically connected to the bottomplate 23, serves as a positive terminal. The negative electrode tab 21is connected to the inner surface of the bottom of the packaging can 16by welding or the like. The packaging can 16 serves as a negativeterminal.

The packaging can 16 is, for example, a closed-end, cylindrical metalcontainer. As described above, the gasket 28 is interposed between thepackaging can 16 and the sealing material 17 to hermetically seal theinternal space of the battery casing 15. The packaging can 16 has agrooved portion 22 that supports the sealing material 17 and is formedby, for example, pressing the side surface from the outside of thepackaging can 16. The grooved portion 22 is preferably formed in aring-like shape in the circumferential direction of the packaging can16. The sealing material 17 is supported by the upper surface of thegrooved portion 22. The upper end of the packaging can 16 is bent inwardand caulked to the periphery of the sealing material 17.

The sealing material 17 has a structure including the bottom plate 23, alower valve plate 24, an insulating member 25, an upper valve plate 26,and a cap 27 which are stacked on top of one another in this order fromclosest to the electrode body 14. The members constituting the sealingmaterial 17 have, for example, a disk-like shape or a ring-like shape.The above members are electrically connected to one another except theinsulating member 25. The lower valve plate 24 and the upper valve plate26 are connected to each other at the centers thereof. The insulatingmember 25 is interposed between the periphery of the lower valve plate24 and the periphery of the upper valve plate 26. In the case where theinternal pressure of the battery is increased due to anomalous heatgeneration, rupturing occurs as a result of the lower valve plate 24becoming deformed to press the upper valve plate 26 upward toward thecap 27 and, consequently, the current pathway between the lower valveplate 24 and the upper valve plate 26 becomes interrupted. If theinternal pressure is further increased, the upper valve plate 26 becomesruptured and the gas is exhausted through the opening of the cap 27.

[Positive Electrode]

The positive electrode 11 includes a positive electrode currentcollector 30 and positive electrode mixture layers 31 disposed on therespective surfaces of the positive electrode current collector 30. Thepositive electrode current collector 30 may be a foil made of a metalstable in the potential range of the positive electrode 11, such asaluminum or an aluminum alloy, a film including a surface layer made ofthe above metal, or the like. The positive electrode mixture layer 31includes a positive electrode active material, a conductive agent, and abinder. The positive electrode 11 may be produced by, for example,applying a positive electrode mixture slurry containing a positiveelectrode active material, a conductive agent, a binder, and the like tothe positive electrode current collector 30, drying the resultingcoating films, and then compressing the coating films to form thepositive electrode mixture layers 31 on the respective surfaces of thepositive electrode current collector 30.

The positive electrode active material includes a lithium metalcomposite oxide as a principal constituent. Examples of the metalelement included in the lithium metal composite oxide include Ni, Co,Mn, Al, B, Mg, Ti, V, Cr, Fe, Cu, Zn, Ga, Sr, Zr, Nb, In, Sn, Ta, and W.Examples of suitable lithium metal composite oxides include a compositeoxide containing at least one element selected from Ni, Co, Mn, and Al.The lithium metal composite oxide may be provided with, for example,particles of an inorganic compound, such as aluminum oxide or alanthanide-containing compound, adhered on the surfaces of particlesthereof.

Examples of the conductive agent included in the positive electrodemixture layer 31 include carbon materials, such as carbon black,acetylene black, Ketjenblack, and graphite. Examples of the binderincluded in the positive electrode mixture layer 31 includefluororesins, such as polytetrafluoroethylene (PTFE) and polyvinylidenefluoride (PVdF), polyacrylonitrile (PAN), a polyimide, an acrylic resin,and a polyolefin. The above resins may be used in combination with acellulose derivative, such as carboxymethyl cellulose (CMC) or a saltthereof, polyethylene oxide (PEO), or the like.

[Negative Electrode]

FIG. 2 is a cross-sectional view of the negative electrode 12. Asillustrated in FIGS. 1 and 2 as an example, the negative electrode 12includes a negative electrode current collector 40, a negative electrodemixture layer 41 (first negative electrode mixture layer) disposed on afirst surface 40 a of the negative electrode current collector 40 whichfaces outward of the electrode body 14, and a negative electrode mixturelayer 42 (second negative electrode mixture layer) disposed on a secondsurface 40 b of the negative electrode current collector 40 which facesinward of the electrode body 14. While the positive electrode 11 has alayer structure including the positive electrode current collector 30and the positive electrode mixture layers 31 that are disposed on therespective surfaces of the positive electrode current collector 30 andidentical to each other, the negative electrode 12 has a layer structureincluding the negative electrode current collector 40 and negativeelectrode mixture layers 41 and 42 that are disposed on the firstsurface 40 a and the second surface 40 b of the negative electrodecurrent collector 40, respectively, and different from each other. Theelectrode mixtures included in the negative electrode mixture layers 41and 42 have different compositions. The details are described below.

The negative electrode current collector 40 may be a foil made of ametal stable in the potential range of the negative electrode 12, suchas copper or a copper alloy, a film including a surface layer made ofthe above metal, or the like. The negative electrode mixture layer 41includes a negative electrode active material and a binder. The negativeelectrode 12 may be produced by, for example, applying a negativeelectrode mixture slurry containing a negative electrode activematerial, a binder, and the like to the negative electrode currentcollector 40, drying the resulting coating films, and then compressingthe coating films to form the negative electrode mixture layer 41 on thefirst surface 40 a of the negative electrode current collector 40 andthe negative electrode mixture layer 42 on the second surface 40 b ofthe negative electrode current collector 40. In the production of thenegative electrode 12, for example, two types of negative electrodemixture slurries may be used.

As illustrated in FIG. 2 as an example, the negative electrode 12constituting the spirally wound electrode body 14 is arranged to curvealong the length thereof in the longitudinal direction. The negativeelectrode 12 is produced in the form of a flat sheet and becomes curvedwhen it is spirally wound together with the positive electrode 11 andthe separator 13 in the production of the electrode body 14. Thenegative electrode 12 commonly has a radius of curvature of about 1 to10 mm. The radius of curvature of the negative electrode 12 variesbetween a winding start-side of the electrode body 14 from which theelectrode body 14 is wound and a winding end-side of the electrode body14 to which the electrode body 14 is wound; the radius of curvature ofthe negative electrode 12 satisfies Winding start-side edge<Windingend-side edge. The minimum radius of curvature of the negative electrode12 is, for example, 1 to 5 mm, or 1 to 2 mm.

Since the negative electrode 12 is produced in the form of a flat sheet,when the negative electrode 12 is curved, the convex-side portion of thenegative electrode 12 is elongated and the concave-side portion of thenegative electrode 12 is compressed. Specifically, the negativeelectrode mixture layer 41 disposed on the first surface 40 a of thenegative electrode current collector 40 which faces outward of theelectrode body 14 is elongated, while the negative electrode mixturelayer 42 disposed on the second surface 40 b of the negative electrodecurrent collector 40 which faces inward of the electrode body 14 iscompressed. The inventors of the present invention successfully enhancedthe cycle characteristics of the battery by improving the layerstructure of the negative electrode 12 focusing on the above point.

The negative electrode mixture layers 41 and 42 have a commonality inthat they include a Si active material composed of at least one of Siand a Si-containing material. The content of the Si active material interms of Si in the negative electrode mixture layer 42 is lower than thecontent of the Si active material in terms of Si in the negativeelectrode mixture layer 41. Since the negative electrode mixture layer42 is compressed as described above, the negative electrode mixturelayer 42 has a smaller margin that allows a great change in the volumeof the Si active material than the negative electrode mixture layer 41.Accordingly, in order to enhance cycle characteristics, it is preferableto satisfy Content of the Si active material in terms of Si in thenegative electrode mixture layer 41>Content of the Si active material interms of Si in the negative electrode mixture layer 42. The content ofthe Si active material in terms of Si is calculated as the ratio of themass of the Si active material included in the negative electrodemixture layer 41 or 42 in terms of Si to the mass of the negativeelectrode active material included in the negative electrode mixturelayer. The mass of the Si active material in terms of Si is calculatedby multiplying the mass of the Si active material by the mass ratio ofSi to the Si active material.

In other words, the content of the Si active material in terms of Si inthe negative electrode mixture layer 41 is set to be higher than thecontent of the Si active material in terms of Si in the negativeelectrode mixture layer 42. Since the negative electrode mixture layer41 is elongated as described above, the negative electrode mixture layer41 has a larger margin that allows a great change in the volume of theSi active material than the negative electrode mixture layer 42.Therefore, increasing the content of the Si active material in thenegative electrode mixture layer 41 is not likely to degrade cyclecharacteristics. Adjusting the contents of the Si active material interms of Si in the negative electrode mixture layers 41 and 42 tosatisfy the above relationship enables the degradation of cyclecharacteristics to be limited while the Si active material is used withefficiency to increase battery capacity.

The layers constituting the negative electrode mixture layers 41 and 42preferably further include a carbon active material. That is, it ispreferable to use the Si active material in combination with a carbonactive material as negative electrode active materials. Although the Siactive material is not necessarily added to the negative electrodemixture layer 42 and may be added to only the negative electrode mixturelayer 41, in this embodiment, the Si active material is added to both ofthe negative electrode mixture layers 41 and 42. From the viewpoint ofcycle characteristics, it is preferable that the content of the Siactive material in each of the negative electrode mixture layers 41 and42 be lower than the content of the carbon active material in thenegative electrode mixture layer. Examples of suitable carbon activematerials include natural graphite, such as flake graphite, lumpgraphite, or amorphous graphite; and artificial graphite, such asmassive artificial graphite (MAG) or graphitized mesophase carbonmicrobeads (MCMB).

The Si active material is composed of at least one of Si and aSi-containing material and is preferably composed of a Si-containingmaterial, which shows a smaller volume change than Si during chargingand discharging. Examples of the Si-containing material include amaterial represent by SiO_(x) (0.5≤x≤1.6). SiO_(x) has a structureconstituted by a SiO₂ matrix and Si microparticles dispersed therein.Alternatively, the Si-containing material may be a material (LSi)constituted by a lithium silicate (Li_(2y)SiO_((2+y)) (0<y<2)) phase andSi microparticles dispersed therein. The negative electrode mixturelayers 41 and 42 may include SiO_(x) and LSi.

It is preferable that a conductive coating composed of a material havinga higher electrical conductivity than the Si-containing material beformed on the surfaces of particles of the Si-containing material.Examples of the material constituting the conductive coating include atleast one selected from a carbon material, a metal, and a metalcompound. In particular, a carbon material, such as amorphous carbon, ispreferable. A carbon coating may be formed by, for example, a CVD methodin which acetylene, methane, or the like is used; or by a method inwhich particles of the Si-containing material are mixed with coal pitch,petroleum pitch, a phenolic resin, or the like and subsequently a heattreatment is performed. Alternatively, the conductive coating may beformed by attaching a conductive filler, such as carbon black, onto thesurfaces of particles of the Si-containing material using a binder. Theamount of the conductive coating is, for example, 0.5% to 10% by mass ofthe mass of particles of the Si-containing material.

The contents of the Si active material in terms of Si in the negativeelectrode mixture layers 41 and 42 satisfy Negative electrode mixturelayer 41>Negative electrode mixture layer 42 as described above. Thedifference in the content of the Si active material in terms of Sibetween the negative electrode mixture layers 41 and 42 is preferably 1%or more, is more preferably 1.5% or more, and is further preferably 2%or more. In such a case, cycle determination may be further markedlyimproved. The contents of the Si active material and the carbon activematerial in terms of Si may be measured by ICP (inductively coupledplasma).

In the case where the Si active material is used in combination with thecarbon active material as negative electrode active materials, thecontents of the Si active material (Si-containing material) in thenegative electrode mixture layers 41 and 42 on a mass basis also satisfyNegative electrode mixture layer 41>Negative electrode mixture layer 42.The content of the Si active material in the negative electrode mixturelayer 41 is preferably 5% to 25% by mass and is more preferably 10% to15% by mass. The content of the Si active material in the negativeelectrode mixture layer 42 is lower than that in the negative electrodemixture layer 41, is preferably less than 15% by mass, and is morepreferably 5% to 10% by mass. The types of the Si active materials addedto the negative electrode mixture layers 41 and 42 may be different fromone another.

The proportion of the Si active material to the negative electrodeactive material in the negative electrode mixture layer 41 is preferably5% to 25% by mass and is more preferably 10% to 15% by mass. Theproportion of the Si active material to the negative electrode activematerial in the negative electrode mixture layer 42 is preferably lessthan 15% by mass and is more preferably 5% to 10% by mass. In otherwords, the proportion of the carbon active material to the negativeelectrode active material in the negative electrode mixture layer 41 ispreferably 75% to 95% by mass. The proportion of the carbon activematerial to the negative electrode active material in the negativeelectrode mixture layer 42 is preferably 85% by mass or more.

Examples of the binder included in the negative electrode mixture layers41 and 42 include a fluororesin, PAN, polyimide, an acrylic resin, and apolyolefin, as in the case for the positive electrode 11. The binderincluded in the negative electrode mixture layers 41 and 42 ispreferably a styrene-butadiene rubber (SBR) or a modifiedstyrene-butadiene rubber. The negative electrode mixture layers 41 and42 may further include, in addition to an SBR and the like, CMC or asalt thereof, polyacrylic acid (PAA) or a salt thereof, polyvinylalcohol, and the like. The types and contents of the binders included inthe negative electrode mixture layers 41 and 42 may be different from oridentical to one another.

The negative electrode mixture layers 41 and 42 may have differentthicknesses and are preferably formed so as to have substantially thesame thickness. The thicknesses of the negative electrode mixture layers41 and 42 may be, for example, 30 to 80 μm and are preferably 40 to 60μm. The negative electrode mixture layers 41 and 42 may further includea negative electrode active material other than the Si active materialor the carbon active material. Examples of the other negative electrodeactive material include a metal other than Si which is capable ofalloying with lithium, a compound containing such a metal, and lithiumtitanate.

[Separator]

The separator 13 may be a porous sheet having ionic permeability and aninsulating property. Specific examples of such a porous sheet include amicroporous thin-film, a woven fabric, and a nonwoven fabric. Examplesof a suitable material for the separator 13 include olefin resins, suchas polyethylene and polypropylene; and celluloses. The separator 13 mayhave either a single-layer structure or a multilayer structure. Theseparator 13 may be provided with a heat-resistant layer or the likedisposed on the surface thereof.

EXAMPLES

The present disclosure is further described with reference to Examplesbelow. The present disclosure is not limited by Examples below.

Example 1 [Preparation of Positive Electrode]

A lithium metal composite oxide represented byLiNi_(0.83)Co_(0.09)Al_(0.03)O₂, carbon black, and polyvinylidenefluoride were mixed with one another at a mass ratio of 100:0.8:0.7. Anappropriate amount of N-methyl-2-pyrrolidone was added to the resultingmixture. Subsequently, the mixture was kneaded. Hereby, a positiveelectrode mixture slurry was prepared. The positive electrode mixtureslurry was applied onto both surfaces of a positive electrode currentcollector composed of an aluminum foil having a thickness of 15 μm.After the resulting coating films had been dried, the coating films wererolled with a roller. Then, the electrode was cut into a predeterminedsize. Hereby, a positive electrode including a positive electrodecurrent collector and positive electrode mixture layers disposed on therespective surfaces thereof was prepared.

[Preparation of First Negative Electrode Mixture Slurry]

A graphite powder was mixed with a Si-containing material represented bySiO_(x) (x=1) having a carbon coating deposited thereon at a mass ratioof 88:12. Hereby, a negative electrode active material was prepared. Thenegative electrode active material, a sodium salt of CMC, andpolyacrylic acid were mixed with one another at a mass ratio of 100:1:1.To the resulting mixture, pure water was added such that the solidcontent was 60% by mass. Then, kneading was performed for 30 minutes.Pure water was added to the kneaded mixture such that the solid contentwas 50% by mass. Subsequently, a dispersion of SBR was added to themixture in an amount equal to 1% by mass of the amount of the negativeelectrode active material. Hereby, a first negative electrode mixtureslurry was prepared.

[Preparation of Second Negative Electrode Mixture Slurry]

A second negative electrode mixture slurry was prepared as in thepreparation of the first negative electrode mixture slurry, except thatgraphite was mixed with the Si-containing material at a mass ratio of92:8.

[Preparation of Negative Electrode]

The first negative electrode mixture slurry was applied onto one of thesurfaces of a negative electrode current collector composed of a copperfoil having a thickness of 8 μm. The resulting coting film was dried toform a first negative electrode mixture layer on the surface of thenegative electrode current collector. Then, the second negativeelectrode mixture slurry was applied onto the other surface of thenegative electrode current collector in an amount equal to the amount ofthe first negative electrode mixture slurry applied. The resultingcoting film was dried to form a second negative electrode mixture layeron the other surface of the negative electrode current collector.Subsequently, the coating films (electrode mixture layers) were rolledwith a roller. Then, the electrode was cut into a predetermined size.Hereby, a negative electrode was prepared. Specifically, the spirallywound electrode body described below was prepared such that the one ofthe surfaces of the current collector served as a first surface facingoutward of the electrode body and the other surface served as a secondsurface facing inward of the electrode body. Table 1 summarizes theproportion of the amount of the Si-containing material to the total massof the negative electrode active material in each of the negativeelectrode mixture layers. In Table 1, the values in the parentheses arethe contents of the Si-containing material in terms of Si in thenegative electrode mixture layers.

[Preparation of Electrode Body]

The positive electrode and the negative electrode were wound around acore having a radius of curvature of 1.5 mm with a separator interposedtherebetween, the separator having a thickness of 20 μm and beingcomposed of a polyethylene microporous membrane. A tape was attachedonto the outermost peripheral surface. Hereby, a cylindrical, spirallywound electrode body was prepared. An aluminum positive electrode leadwas welded to a portion of the positive electrode at which the currentcollector was exposed. A nickel negative electrode lead was welded to aportion of the negative electrode at which the current collector wasexposed.

[Preparation of Nonaqueous Electrolyte]

Ethylene carbonate, dimethyl carbonate, and ethylmethyl carbonate weremixed with one another at a volume ratio of 20:60:20 to prepare a mixedsolvent. Vinylene carbonate was dissolved in the mixed solvent at aconcentration of 2% by mass. Subsequently, LiPF₆ was dissolved in theresulting solution at a concentration of 1.3 mol/liter. Hereby, anonaqueous electrolyte was prepared.

[Preparation of Battery]

The electrode body was inserted into a closed-end cylindrical packagingcan. The positive electrode lead was welded to a sealing material. Thenegative electrode lead was welded to the inner bottom of the packagingcan. After the nonaqueous electrolyte had been charged into thepackaging can, the opening of the packaging can was sealed with thesealing material. Hereby, a nonaqueous electrolyte secondary battery(height: 65 mm, diameter: 18 mm, design capacity: 3500 mAh) wasprepared.

[Evaluation of Cycle Characteristics (Capacity Retention Factor)]

The battery was charged and discharged under the following conditions at25° C. Then, the capacity retention factor of the battery wascalculated. The evaluation results described in Table 1 are relativevalues with the capacity retention factor of the battery prepared inComparative example 1 being 100.

<Charge Discharge Conditions>

Charge: The battery was charged at a constant current of 1050 mA untilthe battery voltage reached 4.2 V. The battery was further charged at aconstant voltage of 4.2 V until the current reached 70 mA.

Discharge: The battery was discharged at a constant current of 1750 mAuntil the voltage reached 2.5 V.

The battery was subjected to 100 cycles of the above charge anddischarge. The capacity retention factor of the battery was calculatedusing the formula below.

Capacity retention factor (%) Discharge capacity in 100thcycle/Discharge capacity in first cycle×100

Example 2

A negative electrode and a nonaqueous electrolyte secondary battery wereprepared as in Example 1, except that the proportion of the amount ofthe Si-containing material to the total mass of the negative electrodeactive material was changed as described in Table 1. The battery wasevaluated in terms of cycle characteristics as in Example 1.

Comparative Example 1

A negative electrode and a nonaqueous electrolyte secondary battery wereprepared as in Example 1, except that the same negative electrodemixture slurry (mass ratio between graphite and Si-containingmaterial=90:10) was used for forming the first and second negativeelectrode mixture layers as described in Table 1. The battery wasevaluated in terms of cycle characteristics as in Example 1.

TABLE 1 Content of Si-containing material (values in parentheses arecontents in terms of Si) First negative Second negative Capacityelectrode mixture electrode mixture retention Factor layer layer(relative value) Example 1 12 mass % 8 mass % 118 (7.6 mass %) (5.1 mass%) Example 2 11 mass % 9 mass % 110 (7 mass %) (5.7 mass %) Comparative10 mass % 10 mass % 100 example 1 (6.4 mass %) (6.4 mass %)

As described in Table 1, the batteries prepared in Examples, where thecontent of the Si active material in terms of Si satisfied Firstnegative electrode mixture layer>Second negative electrode mixturelayer, had a high capacity retention factor and were excellent in termsof cycle characteristics compared with the batteries prepared inComparative example 1. It was confirmed that the cycle characteristicsof the battery prepared in Example 2, where the difference in thecontent of the Si active material between the negative electrode mixturelayers was 2%, was also markedly enhanced.

REFERENCE SIGNS LIST

10 NONAQUEOUS ELECTROLYTE SECONDARY BATTERY, 11 POSITIVE ELECTRODE, 12NEGATIVE ELECTRODE, 13 SEPARATOR, 14 ELECTRODE BODY, 15 BATTERY CASING,16 PACKAGING CAN, 17 SEALING MATERIAL, 18,19 INSULATING PLATE, 20POSITIVE ELECTRODE TAB, 21 NEGATIVE ELECTRODE TAB, 22 GROOVED PORTION,23 BOTTOM PLATE, 24 LOWER VALVE PLATE, 25 INSULATING MEMBER, 26 UPPERVALVE PLATE, 27 CAP, 28 GASKET, 30 POSITIVE ELECTRODE CURRENT COLLECTOR,31 POSITIVE ELECTRODE MIXTURE LAYER, 40 NEGATIVE ELECTRODE CURRENTCOLLECTOR, 40 a FIRST SURFACE, 40 b SECOND SURFACE, 41,42 NEGATIVEELECTRODE MIXTURE LAYER

1. A nonaqueous electrolyte secondary battery comprising a spirallywound electrode body in which a positive electrode and a negativeelectrode are spirally wound with a separator interposed therebetween,wherein the negative electrode includes a negative electrode currentcollector, a first negative electrode mixture layer disposed on a firstsurface of the negative electrode current collector, and a secondnegative electrode mixture layer disposed on a second surface of thenegative electrode current collector, the first surface and the secondsurface facing outward and inward of the electrode body, respectively,wherein the first negative electrode mixture layer includes a Si activematerial composed of at least one of Si and a Si-containing material,and wherein a content of the Si active material in terms of Si in thesecond negative electrode mixture layer is lower than a content of theSi active material in terms of Si in the first negative electrodemixture layer.
 2. The nonaqueous electrolyte secondary battery accordingto claim 1, wherein the second negative electrode mixture layer includesthe Si active material, wherein the content of the Si active material inthe first negative electrode mixture layer is 5% to 25% by mass, andwherein the content of the Si active material in the second negativeelectrode mixture layer is less than 15% by mass.
 3. The nonaqueouselectrolyte secondary battery according to claim 1, wherein the minimumradius of curvature of the negative electrode is 1 to 5 mm.
 4. Thenonaqueous electrolyte secondary battery according to claim 1, whereinthe first negative electrode mixture layer and the second negativeelectrode mixture layer include a carbon active material.